MANAGEMENT RESPONSIBILITY



Similar documents
ISO 9001:2008 Audit Checklist

Quality Manual. UK Wide Security Solutions Ltd. 1 QM-001 Quality Manual Issue 1. January 1, 2011

ISO 9001 (2000) QUALITY MANAGEMENT SYSTEM ASSESSMENT REPORT SUPPLIER/ SUBCONTRACTOR

ISO 9001:2000 AUDIT CHECKLIST

QUALITY MANAGEMENT SYSTEM REQUIREMENTS General Requirements. Documentation Requirements. General. Quality Manual. Control of Documents

CENTRIS CONSULTING. Quality Control Manual

QUALITY MANAGEMENT SYSTEM Corporate

ISO 9001 Quality Systems Manual

FINE LOGISTICS. Quality Manual. Document No.: Revision: A

ISO 9001:2000 Gap Analysis Checklist

Revision Date Author Description of change Jun13 Mark Benton Removed Admin. Manager from approval

QUALITY MANUAL 3 KENDRICK ROAD WAREHAM, MA FAX

Camar Aircraft Products Co. QUALITY MANUAL Revision D

ISO 9001:2008 Quality Management System Requirements (Third Revision)

Micro Plastics, Inc. Quality Manual

The Prophotonix (UK) Ltd Quality manual

QUALITY MANAGEMENT SYSTEMS REQUIREMENTS FOR SERVICE QUALITY BY PUBLIC SERVICE ORGANIZATIONS

23. The quality management system

Quality, Environmental, Health and Safety Manual Toshiba International Corporation

Row Manufacturing Inc. Quality Manual ISO 9001:2008

ISO 9001 : 2008 QUALITY MANAGEMENT SYSTEM AUDIT CHECK LIST INTRODUCTION

QUALITY MANAGEMENT SYSTEM (QMS) ASSESSMENT CHECKLIST

DNV GL Assessment Checklist ISO 9001:2015

Quality Management System Manual

Uncontrolled Document

COMPANY NAME. Environmental Management System Manual

ISO 9001:2008 Clause PR018 Internal Audit Procedure

Rev: Issue 4 Rev 4 Quality Manual AOP0101 Date: 10/07/13. Quality Manual. CBT Technology, Inc. 358 North Street Randolph, MA 02368

Vigilant Security Services UK Ltd Quality Manual

International Workshop Agreement 2 Quality Management Systems Guidelines for the application of ISO 9001:2000 on education.

ISO-9001:2000 Quality Management Systems

Supplier Quality Management System Audit Checklist (ISO 9000:2000, TS 16949:2002)

This Business Management System Manual is based on ISO 9001:2008 requirements

INTEGRATED MANAGEMENT SYSTEM MANUAL IMS. Based on ISO 9001:2008 and ISO 14001:2004 Standards

Quality Manual. Dynamic Manufacturing 156 Armstrong Drive Freeport, PA Revision 6 Revision Date: 7/8/

TOTAL QUALITY MANAGEMENT II QUALITY AUDIT

Quality Systems Manual

QUALITY MANUAL 1. SCOPE, COVERAGE AND BASIS OF QUALITY MANAGEMENT SYSTEM AT APSSDC

QUALITY ASSURANCE MANUAL JPM OF MISSISSIPPI, INC.

ED FAGAN INC. QUALITY SYSTEM MANUAL

QUALITY MANAGEMENT SYSTEM MANUAL

Disclosure to Promote the Right To Information

Free Download ISO/TS 16949:2009. Requirements Checklist. 29 of 57 pages (PDF) For additional information see

IAS ACCREDITED INSPECTION AGENCIES: GUIDELINES FOR CONDUCTING INTERNAL AUDITS AND MANAGEMENT REVIEWS. Revised January, 2016

Contents of the ISO 9001:2008 Quality System Checklist

Doc. No: UPHDB/QM/01 Prepared By: AMR Issue No.:01 Rev. No.: 00 Eff. Date: Page: 1 of 5 Issued by: MR

Quality Manual Printed copy valid for 24 hours from time of printing unless stamped CONTROLLED COPY in red. Page

NABL NATIONAL ACCREDITATION

QUALITY MANUAL ISO Quality Management System

CHECKLIST ISO/IEC 17021:2011 Conformity Assessment Requirements for Bodies Providing Audit and Certification of Management Systems

PAS 99: Integrated Management Systems Checklist IMPLEMENTATION CHECKLIST

Cartel Electronics. AS 9100 Quality Systems Manual

G & R Labs. Quality Assurance Manual. G&R Labs Scott Boulevard Santa Clara CA Light Meters and Calibration

ISO 9001 : 2000 Quality Management Systems Requirements

Company Quality Manual Document No. QM Rev 0. 0 John Rickey Initial Release. Controlled Copy Stamp. authorized signature

Contents. Management Policy Manual SEM USA Page 2 of 12

ISO 9000 Introduction and Support Package: Guidance on the Documentation Requirements of ISO 9001:2008

ISO 9001:2015 Overview of the Revised International Standard

Quality Management System Manual

Audit, Business Risk and Compliance Committee Charter

ISO 9001:2008 QUALITY MANUAL. Revision B

QMS Manual 2350 Helen Street, N. St. Paul, MN Page 1 of 5. Quality Management System Manual

ISO 9001:2008 Quality Manual Clause 3.7.4

a) To achieve an effective Quality Assurance System complying with International Standard ISO9001 (Quality Systems).

Implementing ISO 9000 Quality Management System

IAF Mandatory Document for the Transfer of Accredited Certification of Management Systems

Quality Manual ISO9001:2008

Quality Management System

Quality Manual TABLE OF CONTENTS APPROVAL SIGNATURE PAGE AMENDMENT RECORD SCOPE EXCLUSIONS 2.1 3

Certification Process Requirements

CORPORATE QUALITY MANUAL

ISO 14001:2004 EMS Internal Audit Checklist & Gap Analysis

The President of Inductors Inc. is the senior executive responsible for operations.

Document subject to ISO Requirements

TRANSPORT CANADA MARINE SAFETY PLEASURE CRAFT OPERATOR COMPETENCY PROGRAM QUALITY MANAGEMENT SYSTEM FOR ACCREDITATION

0. 0 TABLE OF CONTENTS

PUBLICATIONS. Introduction

Quality Management System Manual

Turbo Resources International Quality Procedure

ISO 9001:2008 STANDARD OPERATING PROCEDURES MANUAL

MEAT GRADING AND CERTIFICATION BRANCH QUALITY MANUAL

EMS Example Example EMS Audit Procedure

Quality Assurance System Manual

BUSINESS MANAGEMENT SYSTEM MANUAL

Quality Management System Manual

FMC Technologies Measurement Solutions Inc.

ISO 9001: 2008 Boosting quality to differentiate yourself from the competition. xxxx November 2008

Eagle Machining, Inc. Quality Management System

ISO 9001 Quality Management Systems. Tips for Internal Auditing

Quality Management System Process/ Management Review

QUALITY MANAGEMENT SYSTEM (QMS) MANUAL

QUALITY OPERATING PROCEDURE QOP QUALITY ASSURANCE SYSTEM MANUAL

Australian Transport Council. National Standard for the Administration of Marine Safety SECTION 5

AEROSPACE STANDARD. Quality Management Systems - Requirements for Aviation, Space and Defense Organizations RATIONALE

OH&S Management Systems Audit Checklist (NAT, E3)

Quality Manual ALABAMA RESEARCH & DEVELOPMENT. This Quality Manual complies with the Requirements of ISO 9001:2008.

Abu Dhabi EHSMS Regulatory Framework (AD EHSMS RF)

Transcription:

Process Flow: (5.0) Page No. 1 of 7 Management Commitment Customer Focus Quality Policy Quality Planning Quality Objectives System Planning Resource Provision Human Infrastructure Work environment Responsibility Authority and Communication Management Representative Lead Internal Quality Auditor Document Controller Internal Communication Management Review Steering Committee 5.1 MANAGEMENT COMMITMENT: The top management of CRISP, Bhopal is committed to the development and implementation of the quality management system as per ISO 9001:2008 and continually improving its effectiveness by: 1. Communicating to the organization the importance of meeting customer requirements as well as statutory and regulatory requirements. 2. The CRISP organization established as per the Society act and we are following statutory and regulatory requirements as per society act 1973. like o Provident Fund o Income Tax o Minimum wage Act o Gratuity Act as 1972 o Group Insurance o Safety/Electricity Inspection 3. Establishing the quality policy. 4. Establishing the quality objectives. 5. Conducting regular management reviews, and 6. Ensuring the availability of necessary resources.

Page No. 2 of 7 5.2 CUSTOMER FOCUS: Reference: The Top Management ensures that customer requirements are determined and met with the aim to achieve customer satisfaction. 5.3 QUALITY POLICY: Reference: Quality Policy of the Organization is as stated below: "We are committed to provide services like training, consultancy and job-work ensuring customer delight complying with the requirements of our quality management system. We strive for excellence by continuous improvement in all our endeavours." The Quality Policy statement is given wide publicity through prominent display at various locations. Proper understanding of quality policy at all levels is ensured through proper training and direct communication with all employees through appropriate channels. The Quality Policy is reviewed at regular intervals by the management for continuing suitability. 5.4 PLANNING: 5.4.1 Quality Objectives: Quality Objectives are defined and established within the organization and are relevant for the organization. The quality objectives are measurable and are consistent with the Quality Policy. The important quality objectives of the organization are: 1. To ensure compliance of the requirements of ISO 9001: 2000. 2. To strive for continual improvement in the Quality Indices as listed below: Quality Index for Training Effectiveness "QI TE ". ( 87 in One year ) Faculty Index for Training Effectiveness "FI TE ".( 90 in Five years) Training Man-Days "T MD ". (50536 Man Days in two years) Quality Index for Service Quality QI S. (87 In two years ) Quality Index for Product Quality QI P.(87 In two years ) 3. To strive for continual improvement in the processes, people and products through systematic changes ensuring total customer satisfaction.

Page No. 3 of 7 5.4.2 Quality Management System Planning: The top management of the Organization ensures that 1. The planning of the quality management system is carried out in order to meet the requirements given in the products / services as stated in the section (4.0); Clause 4.1 as well as the quality objectives stated above. 2. The integrity of the quality management system is maintained when changes to the quality management system are planned and implemented. 5.5 RESPONSIBILITY, AUTHORITY AND COMMUNICATION: 5.5.1 Responsibility and Authority: 1. The responsibilities of all personnel who manage, perform and verify work-affecting quality and play a designated role in the quality management system are defined in section 9.3; (Annexure - 4) of this Quality Manual. All such designated personnel shall have full authority as may be required to fulfil their responsibilities. 2. The reporting relationship of desired personnel shall be as per documented Organizational Structure (Refer: Section 9.2; Annexure - 3). The functional relationship and interaction shall be in accordance with the relevant operating procedures. 3. In the absence of the designated person, the next senior most person shall carryout all the functions of the designated person as specified under the Line of succession". (Refer: Section 9.3; Annexure - 4). 5.5.2 Management Representative: Mr. Sandeep Sarse Manager (CAD/CAM), a member of the organisation s management has been appointed as the Management Representative and Mr. Piyush Jain Assistant Manager (VLSI) has been nominated as the Dy. Management Representative by the. The Management Representative, in addition to other responsibilities, shall have full responsibility and authority to 1. Ensure that appropriate procedures needed for quality management system are established, documented, implemented and maintained in the Organization. 2. Ensure that the Organization's Quality System meets the requirements of customer and ISO-9001:2008. 3. Report to the Steering Committee on the performance of the quality management system of the Organization and need for improvement. 4. Ensure the promotion of awareness of customer requirements throughout the organization. 5. Verify through planned Internal Quality Audits for continued adherence to these procedures & policies. The Management Representative also does the liaison with the external

bodies on matters related to quality management system. Lead Internal Quality Auditor: Page No. 4 of 7 Mr. Kunjesh Shrivastava Deputy Manager has been nominated as the Lead Internal Quality Auditor by the. The Lead Internal Quality Auditor, in addition to his other responsibilities, shall have full responsibilities and authority to 1. Prepare & issue schedule for Internal Audit in consultation with MR. 2. Guide the IQAs to prepare audit plans and checklists. 3. Organize internal quality audit as per schedule. 4. Prepare summary of IQA reports given by internal auditors. 5. Ensure timely and effective closing of all NCs raised by IQAs. Document Controller: Mr. Alok Dewangan - (I/c Information Centre) has been nominated as the Document Controller by the. The Document controller, in addition to his other responsibilities, shall have full responsibilities and authority to : 1. Prepare Master List of documents and update it regularly. 2. Issue all controlled documents to concerned persons. 3. Withdraw all superseded documents and issue the amended ones. 4. Dispose the obsolete documents appropriately. 5. Keep Master Copy of each document and recording formats. 5.5.3 Internal Communication: The communication within the organization regarding the effectiveness of the quality management system is accomplished in various modes as detailed below: 1. Through notices and circulars on paper. 2. Through LAN system established in various departments. 3. Through meetings at various levels and personal interaction. 4. For administrative purposes the communication is through the. GP 007 5.6 MANAGEMENT REVIEW: 5.6.1 General: 1. Management review meeting are conducted at once in 06 months to ensure suitability, adequacy and effectiveness of the quality management system as per the requirements of ISO-9001: 2008. 2. Management Review includes assessing opportunities for Improvements and need for changes in the quality management system, including quality policy and quality objectives. 3. is responsible for conducting management reviews with the Steering Committee. Management Representative will be the convener of the management review meetings. 4. Records of management reviews are maintained in the form of Minutes of Meeting supported by all necessary forms / charts / graphs etc. annexed to it by the Management Representative.

Page No. 5 of 7 5. Steering Committee The Steering Committee has been constituted by the consisting of the following persons. i) Chairman ii) Secretary & MR - Mr. Sandeep Sarse Manager (CAD/CAM) iii) Dy. MR - Mr. Piyush Jain Assistant Manager (VLSI) iv) Members: AGM (Marketing), Sr. Manager (Comp.& IT), Sr. Manager (Training), Sr. Manager (Info.Centre), Manager (TcPC), Lead Internal Quality Auditor & Document Controller. 5.6.2 Input for Management Review: Management Review shall include information on the following: 1. Results of internal & external quality audits. 2. Feedback from customers and customer complaints. 3. Quality Index for Training Effectiveness "QI TE ". 4. Faculty Index for Training Effectiveness "FI TE ". 5. Training Man-Days "T MD ". 6. Quality Index for Service Quality QI S. 7. Quality Index for Product Quality QI P. 8. Status of Corrective and Preventive actions. 9. Follow-up actions on previous management reviews. 10. Changes that could affect the quality management system. 11. Recommendations for improvement in the system. In addition to the above inputs the review of adequacy / suitability of the following shall also be considered: 1. Quality Policy and Objectives. 2. Documentation. 3. Resources.

Page No. 6 of 7 5.6.3 Output from Management Review: 1. The output of the management reviews include decisions and actions related to the following: a) Improvement of the effectiveness of the quality management system and its processes. b) Improvement of services as per the requirements of the customer and necessary resources needed. 2. Corrective actions as suggested by the Steering Committee and approved by management shall be implemented by respective Department Heads in their functional areas within the target date as decided. Record of such decisions on corrective actions shall be maintained. 3. Implementation of corrective actions decided earlier, if any, shall be reviewed for effectiveness. Effectiveness of reviews and their implementation shall be judged on the basis of reduction in number of non-conformities during internal quality audit and improvement in the indices as stated in the quality objectives. 4. Management Representative may co-opt any Department / Centre Head or their representative for the management review, if the need arises. ************

Page No. 7 of 7